Hereditary dry erythrocytosis

Hereditary xerocytosis (HX) is a rare, autosomal dominant hereditary hemolytic disease, characterized by a dehydrated state of red blood cells and reduced osmotic fragility.

The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.

Was this article helpful? Thanks for the feedback. Thanks for the feedback.